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Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer. [electronic resource] by
- Chappuis, P O
- Hamel, N
- Paradis, A J
- Deschênes, J
- Robidoux, A
- Potvin, C
- Cantin, J
- Tonin, P
- Ghadirian, P
- Foulkes, W D
Producer: 20011004
In:
Clinical genetics vol. 59
Availability: No items available.
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8.
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Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene. [electronic resource] by
- Liu, J
- Fujiwara, T M
- Buu, N T
- Sánchez, F O
- Cellier, M
- Paradis, A J
- Frappier, D
- Skamene, E
- Gros, P
- Morgan, K
Producer: 19950515
In:
American journal of human genetics vol. 56
Availability: No items available.
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9.
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Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population. [electronic resource] by
- Zielenski, J
- Fujiwara, T M
- Markiewicz, D
- Paradis, A J
- Anacleto, A I
- Richards, B
- Schwartz, R H
- Klinger, K W
- Tsui, L C
- Morgan, K
Producer: 19930408
In:
American journal of human genetics vol. 52
Availability: No items available.
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X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis. [electronic resource] by
- Bichet, D G
- Arthus, M F
- Lonergan, M
- Hendy, G N
- Paradis, A J
- Fujiwara, T M
- Morgan, K
- Gregory, M C
- Rosenthal, W
- Didwania, A
Producer: 19931015
In:
The Journal of clinical investigation vol. 92
Availability: No items available.
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